FDA Enforcement Class II Terminated

Galt trephines are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold under the CareFusion brand name.

Recall: Z-0549-2015 · Reported December 17, 2014

Enforcement

Recall Number
Z-0549-2015
Event ID
69471
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Instrumed International, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
December 17, 2014
Initiation Date
September 8, 2014
Classification Date
December 8, 2014
Termination Date
November 29, 2017
Address
626 Cooper Ct, N/A, Schaumburg, IL, 60173-4537, United States

Description

Galt trephines are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold under the CareFusion brand name.

Reason

The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet all FDA requirements to market the devices as "Pre-Amendment" devices.

Code Info

1) Instrumed Product Name: Galt Trephine, 5/8"; Instrumed Product Number: 600-01091; Trade Name: CareFusion; CareFusion Product Name: Galt Trephine, 5/8"; CareFusion Item Number: VM85-1273; Lot Number: 120411.

Distribution

Nationwide Distribution including AZ, CA, FL, IL, KS, MI, NC, OH, PA, TN, TX, and VA.

Quantity

3 Galt trephines